The extracellular matrix in hepatocellular carcinoma Mechanisms and therapeutic vulnerability

被引:13
|
作者
Roy, Arya Mariam [1 ]
Iyer, Renuka [1 ]
Chakraborty, Sayan [1 ,2 ,3 ]
机构
[1] Roswell Pk Comprehens Canc Ctr, Dept Med, Buffalo, NY 14263 USA
[2] Roswell Pk Comprehens Canc Ctr, Dept Pharmacol & Therapeut, Buffalo, NY 14263 USA
[3] Roswell Pk Comprehens Canc Ctr, Program Dev Therapeut, Buffalo, NY 14263 USA
关键词
HEPATIC STELLATE CELLS; POOR-PROGNOSIS; TRANSIENT ELASTOGRAPHY; SERUM-LEVELS; TGF-BETA; T-CELLS; LIVER; EXPRESSION; CANCER; ANGIOGENESIS;
D O I
10.1016/j.xcrm.2023.101170
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The tumor microenvironment (TME) is influenced by a "disorganized"extracellular matrix (ECM) that sensi-tizes cancer cells toward mechanical stress, signaling, and structural alterations. In hepatocellular carcinoma (HCC), lack of knowledge about key ECM proteins driving the TME refractory to targeted therapies poses a barrier to the identification of new therapeutic targets. Herein, we discuss the contributions of various ECM components that impact hepatocytes and their surrounding support network during tumorigenesis. In addi-tion, the underpinnings by which ECM proteins transduce mechanical signals to the liver TME are detailed. Finally, in view of the bidirectional feedback between the ECM, transformed hepatocytes, and immune cells, we highlight the potential role of the ECM disorganization process in shaping responses to immune check-point inhibitors and targeted therapies. Our comprehensive characterization of these ECM components may provide a roadmap for innovative therapeutic approaches to restrain HCC.
引用
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页数:16
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